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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2019
GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon
Tingang Wonkam, E.
;
Chimusa, E.
;
Noubiap, J.J.
;
Adadey, S.M.
;
F Fokouo, J.V.
;
Wonkam, A.
2019
Dietary micronutrient supplementation for 12 days in obese male mice restores sperm oxidative stress
Mc Pherson, N.O.
;
Shehadeh, H.
;
Fullston, T.
;
Zander-Fox, D.
;
Lane, M.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
2018
ADCY9 genetic variants and cardiovascular outcomes with evacetrapib in patients with high-risk vascular disease: a nested case-control study
Nissen, S.
;
Pillai, S.
;
Nicholls, S.
;
Wolski, K.
;
Riesmeyer, J.
;
Weerakkody, G.
;
Foster, W.
;
McErlean, E.
;
Li, L.
;
Bhatnagar, P.
;
Ruotolo, G.
;
Lincoff, A.
2017
Mapping complex traits in a diversity outbred f1 mouse population identifies germline modifiers of metastasis in human prostate cancer
Winter, J.
;
Gildea, D.
;
Andreas, J.
;
Gatti, D.
;
Williams, K.
;
Lee, M.
;
Hu, Y.
;
Zhang, S.
;
Mullikin, J.
;
Wolfsberg, T.
;
McDonnell, S.
;
Fogarty, Z.
;
Larson, M.
;
French, A.
;
Schaid, D.
;
Thibodeau, S.
;
Churchill, G.
;
Crawford, N.
2015
HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouse
Lim, S.
;
Qu, Z.
;
Kortschak, R.
;
Lawrence, D.
;
Geoghegan, J.
;
Hempfling, A.
;
Bergmann, M.
;
Goodnow, C.
;
Ormandy, C.
;
Wong, L.
;
Mann, J.
;
Scott, H.
;
Jamsai, D.
;
Adelson, D.
;
O'Bryan, M.
;
Frye, M.
2013
Influence of aromatase absence on the gene expression and histology of the mouse meibomian gland
Rahimi Darabad, R.
;
Suzuki, T.
;
Richards, S.
;
Jensen, R.
;
Jakobiec, F.
;
Zakka, F.
;
Liu, S.
;
Sullivan, D.
2015
Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity
Moussavi Nik, S.
;
Newman, M.
;
Wilson, L.
;
Ebrahimie, E.
;
Wells, S.
;
Musgrave, I.
;
Verdile, G.
;
Martins, R.
;
Lardelli, M.
2019
DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns
Skvortsova, K.
;
Masle-Farquhar, E.
;
Luu, P.L.
;
Song, J.Z.
;
Qu, W.
;
Zotenko, E.
;
Gould, C.M.
;
Du, Q.
;
Peters, T.J.
;
Colino-Sanguino, Y.
;
Pidsley, R.
;
Nair, S.S.
;
Khoury, A.
;
Smith, G.C.
;
Miosge, L.A.
;
Reed, J.H.
;
Kench, J.G.
;
Rubin, M.A.
;
Horvath, L.
;
Bogdanovic, O.
;
et al.
2011
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases
Lawlor, K.
;
O'Keefe, L.
;
Samaraweera, S.
;
van Eyk, C.
;
McLeod, C.
;
Maloney, C.
;
Dang, T.
;
Suter, C.
;
Richards, R.
Discover
Author
5
et al.
3
Coe, B.
3
Gecz, J.
3
Kvarnung, M.
2
Adelson, D.
2
Friend, K.
2
Hoekzema, K.
2
Liebelt, J.
2
McLeod, C.
2
O'Keefe, L.
.
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Subject
3
Child
3
Gene Expression Regulation, Devel...
3
Genetic Predisposition to Disease
3
Mice, Inbred C57BL
3
Neurons
3
Polymorphism, Single Nucleotide
2
Animals, Genetically Modified
2
Autistic Disorder
2
Case-Control Studies
2
Cohort Studies
.
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